Denecimig denecimig (Mim8) FILED
Drug Profile
ModalityBispecific antibody
RouteSC
Therapy AreaHematology
Peak Sales Est$3000M
Formulations[{"id":"denecimig-sc","notes":"Multiple dosing regimens available (QM, Q2W, QW)","route":"SC","devic
Companies
NVO (LICENSEE)100%
GMAB (ORIGINATOR)0%
Mechanism: FVIIIa mimetic bispecific antibody
Expert: Bispecific antibody bridging FIXa and FX, mimicking the cofactor function of activated FVIII. Enables thrombin generation in the absence of functional FVIII, providing prophylactic hemostasis.
Everyday: Mimics the missing clotting factor (Factor VIII) in hemophilia A. Like a substitute player that does the same job as the missing one, helping blood clot properly.
Targets: []
Programs (1)
IndicationStageKey StudyRegional Status
Hemophilia A +/- inhibitorsFILEDFRONTIER 2/3/4[{"notes":"BLA based on FRONTIER 2/3/4","stage":"FILED","region":"US","filing_da
Notes
FVIIIa mimetic bispecific antibody for hemophilia A prophylaxis. Developed by Novo Nordisk using Genmab DuoBody technology. BLA submitted to FDA Sep 2025 based on FRONTIER 2/3/4 program. Competes directly with Hemlibra (emicizumab, Roche) which had $4.4B 2024 sales.
Data from Supabase · Updated 2026-03-24